(R)-N-Benzyl-1-(naphthalen-1-yl)ethanamine hydrochloride

≥95%

Reagent Code: #113601
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CAS Number 163831-65-0

science Other reagents with same CAS 163831-65-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.82 g/mol
Formula C₁₉H₂₀ClN
badge Registry Numbers
MDL Number MFCD00214135
thermostat Physical Properties
Boiling Point 430.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block in the development of enantioselective catalysts and ligands, which are crucial for asymmetric synthesis. Its structure, featuring a naphthalene group and a benzyl moiety, makes it valuable in the design of compounds with specific stereochemical properties. Additionally, it is employed in the study of receptor interactions and as an intermediate in the synthesis of biologically active molecules, particularly those targeting neurological or cardiovascular systems. Its hydrochloride form enhances solubility, facilitating its use in various experimental and industrial applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,872.00
inventory 250mg
10-20 days ฿3,744.00

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(R)-N-Benzyl-1-(naphthalen-1-yl)ethanamine hydrochloride
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This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block in the development of enantioselective catalysts and ligands, which are crucial for asymmetric synthesis. Its structure, featuring a naphthalene group and a benzyl moiety, makes it valuable in the design of compounds with specific stereochemical properties. Additionally, it is employed in the study of receptor interactions and as an intermediate in the synthesis of biologically active molecules, particularly those targeting neurological or cardiovascular systems. Its hydrochloride form enhances solubility, facilitating its use in various experimental and industrial applications.
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